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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359473Generated: November 3, 2026

Triethylamine → HCID 69110315, compound

https://huagongshe.com/reaction/1359473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantHCID 22145285HCID 22145285—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 69110315HCID 6911031561.3%

Reaction Steps

A mixture of 5-dimethylamino-2-aminotetraline-2-carboxylic acid (1.33 g, 2.15 mmole theoretical), triethylamine (0.40 ml, 2.87 mmole), 9-fluorenylmethyl succinimidyl carbonate (Fmoc-OSu, 0.92 g, 2.73 mmole) in acetonitrile (10 ml) and water (10 ml) was stirred at room temperature for one day. TLC analysis of the reaction indicated the presence of starting material amino acid. 9-fluorenylmethyl succinimidyl carbonate (400 mg) and triethylamine (0.2 ml) were added and the mixture was stirred at room temperature for another day. The reaction mixture was concentrated in vacuo to remove most of the acetonitrile and the almost neutral mixture was extracted three times with ethyl acetate. The combined organic layers were washed with water, brine, dried over sodium sulfate. Filtration and concentration gave a crude which was purified by column chromatography (eluted with 2.5→6→10→15→20% methanol/methylene chloride) to give racemic Fmoc-5-dimethylamino-2-aminotetraline-2-carboxylic acid (602 mg, 61% yield over 2 steps) as an off-white solid. HRMS (FAB): C28H28N2O4 (M) calc. 456.2049; observed: 456.2056.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06600015B2
Source datasetuspto-grants-2003_07
ORD IDord-37960ce68bf34271a8d9427541d8087d
Source noteuspto-grants-2003_07